Treatment tools for endoscope

ABSTRACT

A tubular treatment tool is provided for an endoscope. The tubular treatment tool includes a flexible tubular member. A groove is formed on the flexible tubular member and traverses the flexible tubular member along the diameter. An operation wire is provided in the flexible tubular member. The operation wire is movable relative to the flexible tubular member along an axis of the flexible tubular member. A distal end of the operation wire is secured to the flexible tubular member at a position on a distal end side with respect to the groove. A tissue collecting device is secured at the distal end of the flexible tubular member.

This application is a continuation of U.S. patent application Ser. No.10/081,854, filed on Feb. 25, 2002, which is now U.S. Pat. No. 6,814,728issued on Nov. 9, 2004, the disclosure of which is expresslyincorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION

The present invention relates to a measurement tool or treatment toolfor an endoscope.

A measurement tool for an endoscope is typically used for measuring asize of an ulcer or the like on a mucous membrane in a human cavity. Themeasurement tool is generally configured such that graduations areformed at a tip end portion of a flexible shaft, which is detachablyinserted through an instrument tool insertion channel of the endoscope.An example of such a measurement tool is disclosed in Japanese UtilityModel Publication HEI 6-44401.

With the measurement tool configured as described above, a size only inone direction can be measured, and a length in another direction cannotbe measured. In order to measure the size of an object in two differentdirection, a direction where the graduations are provided should bechanged. However, at the tip of the endoscope, at which a positionalrelationship with respect to the ulcer is limited, it is difficult tochange the orientation of the distal end of the endoscope. Thus, it isalmost impossible to directly measure the length of the object (e.g.,ulcer) in two different directions. Therefore, a length in one directionshould be guessed based on the measured length.

The Japanese Utility Model Publication HEI 6-44401 teaches a measurementtool provided with a flexible tube having two slits, which traverse theflexible tube in the diameter direction, at a certain interval along theaxis of the flexible tube. By operation an operation wire, the distalend portion of the flexible tube, on which gradations are formed, isbent to form a T-shape. However, in such a configuration, the flexibletube is bent by 180 degrees at one of the two slits. Therefore, whensuch a bending operation is repeated, the flexible tube may be broken,at the slit, within a relatively short period of time.

Another typical tool for an endoscope is an injection tube for injectingcontrast medium. A conventional injection tube is typically formed as asingle tube made of flexible resin such as tetrafluoroethylene. Aninjection mouth is provided at the proximal end of the injection tube.At the distal end thereof, an end tip may be secured. In some injectiontubes, a core metal is inserted so that the tube is not folded.

The tubular tool as described above is inserted in a treatment toolchannel of an endoscope. In the conventional treatment tool, anorientation or a direction of a distal end portion of the tubular tool,which is protruded from the distal end of the endoscope, cannot becontrolled. Therefore, according to the conventional art, the distal endportion of the flexible tube is formed to have tendency to bend in apredetermined direction. Even with such a tubular tool, it is stilldifficult to insert the tubular tool in a diverging tube at a deepportion of a bile duct or bronchial tubes.

Another typical treatment tool for an endoscope is a bendable treatmenttool used for collecting tissues from a mucous membrane inside a humancavity.

As such treatment tools for collecting human tissues, ones having abrush tool or spoon tool are secured onto a tip end of a flexiblybendable sheath. An example of such a tool is described in JapanesePatent Provisional Publication HEI 05-142.

Conventional tools for collecting human tissues, as described in theabove-described publication, are configured as precision instrument suchthat link members rotatable at respective rotation axes, which areperpendicular to the axis of the flexible tube, are provided at the tipend portion of the flexible sheath. The link members are configured tobe bent/expanded upon back/forth movement of an operation wire.

With this precise structure, it is difficult to clean the toolcompletely after operation thereof. Further, due to the precisestructure, the tool easily malfunctions. Due to the precise structure,such tools are relatively expensive and may not be disposable.Accordingly, the conventional tools may be reused in unstable condition.

Another typical treatment tool for an endoscope is a catheter, which isinserted in the forceps channel of an endoscope, and is used for feedingof chemicals or suction of bodily fluids.

The catheter for an endoscope is generally formed of a flexible tubehaving a simple structure. In order to lead the distal end of thecatheter to a target position, it is preferable that the direction ofthe distal end portion is remotely changeable.

FIG. 35 shows a structure of a conventional catheter for an endoscope.As shown in FIG. 35, the conventional catheter includes a flexible tube501. Inside the flexible tube 501, an operation wire 502 is looselyinserted. At the distal end portion of the flexible tube 1, a pair ofholes 503 are formed, which are spaced along the axial direction by apredetermined amount. Between the holes 503, the operation wire 502 islocated outside the flexible tube 501 and extends along the axis of theflexible tube 501. Further, the flexible tube 1 is provided with aplurality of circumferential grooves 504 at a predetermined interval sothat the flexible tube 1 is easily bent.

In the catheter configured as described above, if the operation wire 502has tendency to bend in a certain direction, the flexible tube 1 maymeander. In such a case, the catheter cannot be used. Therefore,generally twisted wires having less rigidity are used as the operationwire 502.

When the operation wire 2 is pulled, the distal end portion of theflexible tube 501 is bent as indicated by two-dotted lines in FIG. 35.However, even if the operation wire is pushed, due to its low rigidity,the distal end portion of the flexible tube 1 may not bend. Thus,according to the conventional structure, it is very difficult to leadthe distal end of the catheter to a desired direction.

A cytodiagnosis brush is known as treatment tool for an endoscope.Generally, the cytodiagnosis brush is configured such that a brush shaftprovided with radially planted brush at the distal end portion thereofis connected with the distal end of a closely wounded coil pipe, whichcan be inserted in the treatment tool insertion channel of theendoscope.

Endoscopes should be cleaned and disinfected completely after they areused. However, for the cytodiagnosis brush described above, it isdifficult to completely clean and disinfect inside the coil pipe.Therefore, in order to avoid contagion between patients via thecytodiagnosis brush, it must be disposed when it is used once, which hasbeen considered wasteful.

Another typical treatment tool for an endoscope is a biopsy forceps forcollecting biopsy tissues from the human cavity.

The biopsy forceps is generally configured such that an operation wireis movably inserted in a flexible sheath, and by moving the operationwire, a pair of forceps cups provided at the distal end of the flexiblesheath are opened/closed.

In a conventional biopsy forceps configured as above, the direction ofthe distal end portion of the sheath cannot be changed. FIG. 46schematically shows a branched portion of a brachial tube, in which anendoscope 750 is inserted. In FIG. 46, 701 denotes a flexible sheath and702 denotes forceps cups. In this example, the endoscope should beinserted to a branched tube having a tumor 100. However, since thedirection of the distal end portion of the flexible sheath 701 cannot bechanged, when the flexible sheath 701 is protruded from the distal endof the endoscope, the flexible sheath enters the other tube as shown inFIG. 47.

Even if the flexible sheath 701 can be introduced in the desired tube,as shown in FIG. 48, the tissues are collected with the forceps cups 702abutting against the tumor 100 from the side. Therefore, invasion areaof malignant lesion may not be diagnosed accurately.

In Japanese Utility Model Publication SHO 52-33146 or Japanese PatentPublication SHO 53-10396, a biopsy forceps having a mechanism to bendthe flexible sheath at the distal end portion thereof is described.However, if the sheath is very thin, such a mechanism cannot bepractically employed in view of the strength and operability.

A further typical treatment tool for an endoscope is a high-frequencycutting tool used for cutting human tissues using a high-frequency.

FIG. 52 shows a structure of a conventional high-frequency cutting toolfor an endoscope. As shown in FIG. 52, the conventional high-frequencycutting tool includes a flexible tube 801 made of electricallyinsulating material. Inside the flexible tube 801, a conductive wire 802is loosely inserted. At the distal end portion of the flexible tube 801,a pair of holes 803 are formed, which are spaced along the axialdirection by a predetermined amount. Between the holes 803, theconductive wire 802 is located outside the flexible tube 801 and extendsalong the axis of the flexible tube 801. Further, the flexible tube 801is provided with a plurality of circumferential grooves 804 at apredetermined interval so that the flexible tube 1 is easily bent. Sucha structure is disclosed in Japanese Patent Publication SHO 64-4335.

By pulling the conductive wire as indicated by arrow in FIG. 52, thedistal end portion of the flexible tube 1 between the pair of holes 803is bent as indicated by two-dotted lines in FIG. 52.

FIG. 51 shows a usage of the high-frequency cutting tool describedabove. The distal end portion of the flexible tube 1 is inserted in anopening of bile duct 102 communicating with the duodenum 101, and thehigh-frequency current is applied to the conductive wire 802. Then, thetissues at the opening are cut. In FIG. 51, 850 denotes the endoscopeand 851 denotes the treatment tool channel of the endoscope 850.

In the conventional high-frequency cutting tool as described above, thebending amount of the distal end portion of the flexible tube 801 isdetermined only by the pulling force of the conductive wire 802, and inaccordance with the bending amount, the cutting depth 800A of thetissues is determined.

However, the bending amount cannot be controlled accurately, andtherefore, the cutting depth 800A may not be different from the intendedamount.

SUMMARY OF THE INVENTION

According to some embodiments of the invention, there is provided ameasurement tool for an endoscope, with which a two-dimensional size ofan object such as an ulcer can be measured relatively easily andaccurately.

According to some embodiments of the invention, there is provided atubular treatment tool for an endoscope, which is configured such thatthe orientation of the distal end portion thereof can be changedarbitrarily with operation of an operation unit, and can be inserted inthe diverging tube located deep inside the bile duct or bronchial tubes.

According to some embodiments of the invention, there is provided abendable treatment tool for an endoscope, which has a relatively simplestructure. Because of the simple structure, the tool may be cleanedeasily, and is hard to malfunction. Further, due to its simplestructure, the tool may be manufactured at a relatively low cost, andthus can be provided as a disposable tool.

According to some embodiments of the invention, there is provided ameasurement tool for an endoscope, which has a relatively highdurability, and can be manufactured at a relatively low manufacturingcost.

According to one embodiment of the invention, there is provided acatheter for an endoscope operable with an operation wire. The distalend portion of the catheter may be bent not only by pulling theoperation wire but also pushing the operation wire so that the distalend portion of the flexible tube can be directed in a desired direction.

According to some embodiments of the invention, there is provided acytodiagnosis brush which can be cleaned and disinfected completelyafter usage, and can be used repeatedly without contagion amongpatients.

According to some embodiments of the invention, there is provided abiopsy forceps, a direction of the distal end portion of which can bechanged without employing a complicated mechanism and/or operation.

According to one embodiment of the invention, there is provided ahigh-frequency cutting tool with which the bending amount of the distalend portion of the flexible tube is controlled accurately so that thecutting amount can be adjusted to the desired amount.

In view of the above, according to the invention, there is provided ameasurement tool for an endoscope, which is provided with a flexibleshaft to be inserted in a treatment tool insertion channel of theendoscope, and an elastic sheet member secured to a distal end portionof the flexible shaft.

Optionally, the distal end portion of the flexible shaft may be bendableat a position on the proximal end side with respect to the elastic sheetmember, the distal end portion of the flexible shaft being bendable inresponse to an operation at a proximal end of the flexible shaft.

Further optionally, the sheet member may include a substantiallycircular sheet.

In this case, the sheet member may include a plurality of sheets havingdifferent diameters, the plurality of sheets being secured to theflexible shaft at different positions.

The graduations may be formed on the sheet member.

In a particular case, the sheet member may be detachably secured to theflexible shaft.

The measurement tool may further include an elastic annular sheetsecured to the flexible shaft, the annular sheet surrounding the sheetmember.

According to another aspect, there is provided a tubular treatment toolfor an endoscope, which includes a flexible tubular member, a groovetraversing the flexible tubular member in a direction of a diameterthereof being formed, and an operation wire inserted in the flexibletubular member, the operation wire being movable relative to theflexible tube along an axis of the flexible tube, a distal end of theoperation wire being secured to the flexible tube at a position on adistal end side with respect to the groove.

Optionally, the groove may have a V-shaped cross section.

Further, a tissue collecting device may be secured at the distal end ofthe flexible tube.

According to a further aspect of the invention, there is provided atubular treatment tool for an endoscope, which includes a flexibletubular member, at least one pair of grooves each traversing theflexible tubular member in a direction of a diameter thereof beingformed, and an operation wire inserted in the flexible tubular member,the operation wire being movable relative to the flexible tube along anaxis of the flexible tube, the operation wire running outside of thetubular member through one of the pair of grooves and running inside ofthe tubular member so that the operation wire is located outside of theflexible tubular member between the pair of grooves, a distal end of theoperation wire being secured to the flexible tube at a position on adistal end side with respect to the pair of grooves.

Optionally, each of the grooves may have a V-shape cross section.

Further optionally, at least one pair of grooves may include a pluralityof pairs of grooves, the operation wire being located outside of theflexible tubular member between two grooves of each pair of theplurality of pair of grooves.

In this case, the plurality of pairs of grooves may be located atdifferent positions along the circumference of the flexible tubularmember.

Still optionally, a tissue collecting device may be secured at thedistal end of the flexible tube.

According to another aspect of the invention, there is provided ameasurement tool for an endoscope, which is provided with a flexibletubular member, a groove traversing the flexible tubular member in adirection of a diameter thereof being formed, at least a distal endside, with respect to the groove, of the flexible tubular member beingformed with graduations, and an operation wire inserted in the flexibletubular member, the operation wire being movable relative to theflexible tube along an axis of the flexible tube, a distal end of theoperation wire being secured to the flexible tubular member at aposition on a distal end side with respect to the groove.

Optionally, the groove may have a V-shaped cross section.

Still optionally, a fluid injection mouth, which communicates with theflexible tubular member, may be provided at a proximal end portion ofthe flexible tubular member.

According to a further aspect of the invention, there is provided acatheter for an endoscope, which is provided with a flexible tubularmember through which fluid passes, a groove traversing the flexibletubular member in a direction of a diameter thereof being formed, thegroove having a V-shaped cross section, and an operation wire insertedin the flexible tubular member, the operation wire being movablerelative to the flexible tube along an axis of the flexible tube, adistal end of the operation wire being secured to the flexible tubularmember at a position on a distal end side with respect to the groove, apair of holes being formed on both sides, along an axis of the flexibletubular member, of the groove, the operation wire being inserted throughthe pair of holes so that the operation wire being located outside ofthe flexible tubular member at a position between the pair of holes.

According to a further aspect of the invention, there is provided acytodiagnosis brush for an endoscope, which is provided with a flexibletubular member, a brush shaft, a brush being radially planted at adistal end portion of the brush shaft, and a stopper secured to theproximal end of the brush shaft, the stopper being fixed to the flexibletubular member at a distal end portion thereof, a fluid passage along anaxis of the flexible tubular member being defined in the stopper.

Optionally, a groove traversing the flexible tubular member in adirection of a diameter thereof may be formed, the groove having aV-shaped cross section, and the cytodiagnosis brush further comprises anoperation wire inserted in the flexible tubular member, the operationwire being movable relative to the flexible tube along an axis of theflexible tube, a distal end of the operation wire being secured to theflexible tubular member at a position on a distal end side with respectto the groove, a pair of holes being formed on both sides, along an axisof the flexible tubular member, of the groove, the operation wire beinginserted through the pair of holes so that the operation wire is locatedoutside of the flexible tubular member at a position between the pair ofholes.

According to another aspect of the invention, there is provided a biopsyforceps for an endoscope, which is provided with a flexible tubularmember, an operation wire inserted through the flexible tubular member,a pair of forceps cups secured to the distal end of the flexible tubularmember, a link mechanism with which the pair of forceps cups open andclose upon operation of the operation wire, an incision being formed,from an outer surface of the flexible tubular member, at a distal endportion of the flexible tubular member along a direction of a diameterof the flexible tubular member.

Optionally, an end of the incision may be located substantially at aposition past the inner diameter of the flexible tubular member.

In a particular case, the incision is a slit. Alternatively, theincision may be a groove having a V-shaped cross section.

According to a further aspect of the invention, there is provided ahigh-frequency cutting tool for an endoscope, which is provided with anelectrically insulating flexible tubular member, at least one pair ofgrooves each traversing the flexible tubular member in a direction of adiameter thereof being formed, and a conductive wire inserted in theflexible tubular member, the conductive wire being movable relative tothe flexible tube along an axis of the flexible tube, wherein a groovetraversing the flexible tubular member in a direction of a diameterthereof is formed, the groove having a V-shaped cross section, a distalend of the conductive wire being secured to the flexible tubular memberat a position on a distal end side with respect to the groove, a pair ofholes being formed on both sides, along an axis of the flexible tubularmember, of the groove, the conductive wire being inserted through thepair of holes so that the operation wire is located outside of theflexible tubular member at a position between the pair of holes.

BRIEF DESCRIPTION OF THE ACCOMPANYING DRAWINGS

FIG. 1 is a side view of a distal end portion of a measurement tool foran endoscope according to a first embodiment of the invention;

FIG. 2 is a cross-sectional side view of a distal end portion of themeasurement tool according to the first embodiment;

FIG. 3 is a cross-sectional view taken along line III-III of FIG. 2;

FIG. 4 shows the measurement tool in use according to the firstembodiment;

FIG. 5 is a side view of a distal end portion of a measurement tool foran endoscope according to a second embodiment of the invention;

FIG. 6 is a cross-sectional side view of a distal end portion of themeasurement tool according to the second embodiment;

FIG. 7 is a cross-sectional side view of a distal end portion of themeasurement tool according to the third embodiment;

FIG. 8 is a cross-sectional side view of a distal end portion of themeasurement tool according to the fourth embodiment;

FIG. 9 is a cross-sectional side view of a tubular treatment tool for anendoscope according to a first embodiment of the invention;

FIG. 10 is a cross-sectional side view of a distal end portion of thetubular treatment tool when the distal end portion is bent;

FIG. 11 is a cross-sectional side view of the distal end portion of thetubular treatment tool when the distal end portion is bent in adirection opposite to that shown in FIG. 2;

FIG. 12 illustrates the tubular treatment tool in use;

FIG. 13 shows an operation wire fixing structure of a tubular treatmenttool according to a second embodiment;

FIG. 14 shows a groove of a tubular treatment tool according to a thirdembodiment of the invention;

FIG. 15 shows a groove of a tubular treatment tool according to a fourthembodiment of the invention;

FIG. 16 shows a tubular treatment tool according to a fifth embodimentof the invention, a spoon being secured to the tip thereof;

FIG. 17 shows a tubular treatment tool according to a sixth embodimentof the invention, a brush being secured to the tip thereof;

FIG. 18 is a cross-sectional side view of a distal end portion of abendable treatment tool according to a first embodiment of theinvention;

FIG. 19 is a cross-sectional side view of the distal end portion of thebendable treatment tool according to the first embodiment when thedistal end portion is bent in one direction;

FIG. 20 is a cross-sectional side view of the distal end portion of thebendable treatment tool according to the first embodiment when thedistal end portion is bent in another direction;

FIG. 21 is a cross-sectional side view of a distal end portion of abendable treatment tool according to a second embodiment of theinvention;

FIG. 22 is a side view of a distal end portion of a bendable treatmenttool according to a third embodiment of the invention;

FIG. 23 is a side view of the distal end portion of the bendabletreatment tool according to the third embodiment when the distal endportion is bent;

FIG. 24 is a partially cross-sectional side view of a measurement toolfor an endoscope according to a first embodiment of the invention;

FIG. 25 is a partially cross-sectional side view of a distal end portionof the measurement tool according to the first embodiment, when thedistal end portion is bent;

FIG. 26 shows the measurement tool according to the first embodiment,when in use;

FIG. 27 shows the measurement tool according to the first embodimentwhen in use;

FIG. 28 shows the measurement tool according to the first embodimentwhen in use;

FIG. 29 shows grooves formed on a measurement tool according to a secondembodiment;

FIG. 30 is a partially cross-sectional side view of a distal end portionof the measurement tool according to a third embodiment;

FIG. 31 shows a measurement tool according to a fourth embodiment, whenin use;

FIG. 32 is a partially cross-sectional side view of a catheter for anendoscope according to a first embodiment of the invention;

FIG. 33 is a cross-sectional view taken along line B-B of FIG. 32;

FIG. 34 shows a cross-sectional side view of the catheter according tothe first embodiment, when the distal end portion is bent;

FIG. 35 shows a cross-sectional side view of a conventional catheterwhen the distal end portion thereof is bent;

FIG. 36 is a cross-sectional side view of a distal end portion of acytodiagnosis brush according to a first embodiment of the invention;

FIG. 37 is a cross-sectional view taken along line C-C of FIG. 36;

FIG. 38 is a partially cross-sectional side view showing an entirestructure of the cytodiagnosis brush according to the first embodiment;

FIG. 39 is a cross-sectional side view showing an entire structure of acytodiagnosis brush according to a second embodiment;

FIG. 40 is a cross-sectional side view of the distal end portion of thecytodiagnosis brush according to the second embodiment;

FIG. 41 is a cross-sectional side view showing a distal end portion of abiopsy forceps according to a first embodiment when it is bent;

FIG. 42 is a cross-sectional side view showing a distal end portion of abiopsy forceps according to the first embodiment when it isstraightened;

FIG. 43 schematically shows the biopsy forceps according to the firstembodiment when in use;

FIG. 44 schematically shows the biopsy forceps according to the firstembodiment when in use;

FIG. 45 is a cross-sectional side view showing a distal end portion of abiopsy forceps according to a second embodiment;

FIG. 46 schematically shows the conventional biopsy forceps when in use;

FIG. 47 schematically shows the conventional biopsy forceps when in use;

FIG. 48 schematically shows the conventional biopsy forceps when in use;

FIG. 49 is a cross-sectional side view of a distal end portion of ahigh-frequency cutting tool according to an embodiment of the invention;

FIG. 50 is a cross-sectional side view of the distal end portion of thehigh-frequency cutting tool according to the embodiment of theinvention, when it is bent;

FIG. 51 schematically shows the high-frequency cutting tool when in use;and

FIG. 52 is a cross-sectional side view of a distal end portion of aconventional high-frequency cutting tool.

DETAILED DESCRIPTION OF THE EMBODIMENTS

Hereinafter, embodiments according to the present invention will bedescribed with reference to the accompanying drawings.

FIRST-FOURTH EMBODIMENTS

FIG. 1 is a side view of a distal end portion of a flexible shaft 1which is to be inserted in an endoscopic instrument insertion channel ofan endoscope. FIG. 2 is a cross-sectional side view of the flexible tube1, and FIG. 3 is a cross-sectional view taken along line III-III of FIG.2. For example, an outer diameter of the flexible shaft 1 isapproximately 2 mm, which is formed by a coil pipe made of a stainlesssteel wire. Specifically, the flexible shaft 1 includes a flexible body1 a whose length is one to two meters, and a bendable portion 1 b whichis a proximal end portion. The flexible body 1 a and the bendableportion 1 b are connected via a link mechanism 2.

Through the flexible body 1 a, an operation wire 3 is inserted along theaxis of the flexible body 1 a. An operation unit of the endoscope isconnected with the proximal end of the flexible body 1 a of the flexibletube 1. The operation wire 3 is movable in forward/backward direction inresponse to an operation of the operation unit.

By operating the operation wire 3 to move toward the proximal end (whichwill be referred to as a backward movement), the bendable portion 1 brotates about a shaft 2 a of the link mechanism 2, and the flexible tube1 is bent at the link mechanism 2 as best seen in FIG. 2. The maximumbendable angle θ is preferably within a range of 30° to 120°. Morepreferably, the maximum bendable angle θ may be approximately 90°.

At an intermediate portion, along the axis, of the bendable portion 1 b,a circular sheet 5, whose diameter is 2-10 mm is secured. The sheet 5 ismade of elastic material such as a silicon rubber sheet which reformsits shape to a sheet like one after certain period of time even if it isbent.

It should be noted that the sheet 5 need not be limited to one formed ofsilicon rubber. One formed of synthetic resin such as polyethylene,polyamide or the like can by used. If sufficient elasticity is achieved,a kind of paper may also be used.

It is preferable that the sheet 5 has a color different from the colorof the surface of the mucous membrane. Preferably, the color is non-red(including white). It may be convenient to use a half-transparentmaterial, since the object can be observed through the half-transparentsheet.

As shown in FIG. 3, the sheet 5 is adhered onto the bendable portion 5such that the central portion of the sheet 5 surrounds the outercircumferential surface of the bendable portion 1 b. A plane in whichthe bendable portion 1 b bends is substantially perpendicular to thesurface of the sheet 5.

The measurement tool thus configured is inserted in the tool channelwith the bendable portion 1 b straightened with respect to the flexiblebody 1 a as shown by solid line in FIG. 1. It should be noted that, whenthe measurement tool is inserted in the treatment tool channel, thesheet 5 is bent or folded so that the sheet 5 can pass through theinsertion channel.

When the bendable portion 1 b is protruded from the distal end of theinsertion channel, the sheet 5 restores its original shape due to itselasticity. Further, the bendable portion 1 b can be bent by operatingthe operation wire 3 at the operation unit as shown in FIG. 2. Thus, thesheet 5 can be located in front of an observation field A.

By moving the flexible shaft 1 toward the ulcer 100 so that the sheet 5is located closely adjacent to the ulcer 100, the two-dimensional sizeof the ulcer 100 can be measured using the gradations on the sheet 5.

FIG. 5 shows the tip portion of a measurement tool according to thesecond embodiment. In the second embodiment, the flexible tube 1 isformed of tetrafluoroethylene resin. Instead of the link mechanism 2employed in the first embodiment, a V-shaped groove 6 is formed in adirection of the diameter of the flexible tube 1. The tip end of theoperation wire 3 is fixed to the bendable portion 1 b. Therefore, if theoperation wire 3 is pulled (i.e., moved backward), the flexible tube 1bends at the V-shaped groove 6.

Further, a plurality of sheets 5 having different diameters are securedto the bendable portion 1 b at different axial positions. With thisconfiguration, a suitable one of the sheets 5 can be used in accordancewith the size of the ulcer 100.

It should be noted that, although the sheet having a larger diameter isprovided on the distal end side of the bendable portion 1 b in FIG. 5,ones having smaller diameters may be arranged on the distal end side.

Furthermore, in the second embodiment, as shown in FIG. 6, the sheet 5is formed with a cylindrical through opening 5 a and elastically fittedon a smaller-diameter portion of the bendable portion 1 b. With thisconfiguration, each sheet 5 can be rotated about the axis of thebendable portion 1 b.

Therefore, even though the flexible shaft 1 should be inserted obliquelytoward the ulcer 100, the sheet 5 can be oriented in parallel with thesurface of the mucous membrane, which enables accurate measurement.

Optionally, as shown in FIG. 7, the sheet 5 may be provided withgradations 7. Further optionally, the cylindrical through opening 5 bmay be formed to have tapered shape having a larger diameter at theaxial end side, so that the sheet 5 can be detached from the bendableportion 1 b.

Still optionally, an annular sheet 5A, which is formed of elasticmaterial, may be provided substantially co-centrically with respect tothe sheet 5 (see FIG. 8). With this configuration, a measurable rangecan be enhanced.

FIFTH-TENTH EMBODIMENTS

FIG. 9 shows a tubular treatment tool for an endoscope according to afirst embodiment of the invention.

In FIG. 9, 201 denotes a flexible tube to be inserted in a treatmenttool insertion channel. The flexible tube 1 is a tetrafluoroethyleneresin tube or polyethylene resin tube, the outer diameter thereof being1.5 to 2.5 mm, and the length thereof being 1 to 2 meters.

At the tip end portion of the flexible tube 201, a groove 203 having aV-shaped cross section. Inside the flexible tube 1, an operation wire202 which is formed of, for example, twisted stainless steel wires, areinserted along the axis thereof over the length thereof. The operationwire 202 is movable along the axis of the flexible tube 201.

At the tip end of the flexible tube 201, a metal chip 204 having athrough hole in the axial direction is secured. The tip end of theoperation wire 202 is secured to the inner circumference of the metalchip 204 by silver brazing or the like. Thus, the tip end of theoperation wire 202 is fixed to the tip end portion of the flexible tube201.

The treatment tool 210 is provided with an operation unit 210. Theoperation unit 210 includes a main barrel 211 to which the proximal endof the flexible tube 201 is connected. From the main barrel 211, aconnection barrel 212 is protruded. By connecting an injector (notshown) to the connection barrel 212, contrast medium or other liquid canbe fed through the flexible tube 201. Further, through the flexible tube201, suction can be done.

The operation wire 202 runs through the main barrel 211, and the rearside end of the main barrel 211 is connected with a finger hook 214. Theportion of the operation wire 202 from the main barrel 211 to the fingerhook 214, a reinforcement pipe 215 made of stainless steel is providedto cover the operation wire 202.

With the above-described configuration, by moving the finger hook 214back and forth with respect to the main barrel 11, the operation wire202 moves back and forth, along the axis, inside the flexible tube 201.In FIG. 9, 213 denotes an O-ring which is used for sealing a spaceinside the main barrel 211 and outside of the main barrel 211. TheO-ring 213 closely contacts the outer circumference of the reinforcepipe 215.

When the operation wire 202 is pulled (i.e., moved backward) by movingthe finger hook 213 in a rear direction (i.e., right-hand side directionin FIG. 9), then, as shown in FIG. 10, the tip end portion of theflexible tube 201 bends toward the groove 203 such that the V-shapedcross section becomes smaller. In an example shown in FIGS. 9 and 10,the maximum bendable angle is set to 90 degrees. It should be noted thatthe maximum bendable angle is adjusted by setting an angle formedbetween both sides of the V-shape cross section of the groove 203.

When the operation wire 202 is pushed (i.e., moved forward) by movingthe finger hook 214 in a forward direction (i.e., left-hand sidedirection in FIG. 9), then, as shown in FIG. 11, the tip end portion ofthe flexible tube 201 bends in a direction opposite to the groove 203.

Thus, with the tubular treatment instrument for an endoscope accordingto this embodiment, the tip end portion (e.g., metal chip 204) of theflexible tube 201, which is protruded from the distal end of theinsertion channel 251 of an endoscope 60 (see FIG. 12), can be bent in adesired direction so that the tip end portion can be inserted in abranch tube located at a relatively deep level of bronchial tubes or abile duct. Generally, such portions cannot be observed by eyes, andcontrast medium may be injected and X-ray observation may be performed.

The present invention is not limited to above-described configuration,and may be modified in various ways. For example, the metal chip 204 maybe secured to the tip end of the operation wire 202 in various ways.

In FIG. 13, a metal chip 204M is formed to have a heart shape, and thetip end of the operation wire 202 is secured at the concave portion ofthe outer surface of the metal chip 4M. Then, the metal chip 204M,together with the operation wire 202, is press-fixed inside the tip endportion of the flexible tube 1.

In FIG. 14, a modification of the groove 203 is shown. In thismodification, the cross-sectional shape of the groove 203 is modifiedsuch that the summit of the upended V-shape has a predetermined lengthof a level portion. With this configuration, the flexible tube 201 mayeasily bend in response to operation of the operation wire 202.

In FIG. 15, the groove 203 is formed such that an operation unit side ofthe V-shaped cross-section inclines steeply, and a tip end side of theV-shaped cross-section gently inclines. With this configuration, whenthe flexible tube 201 is retracted and the tip end portion of theflexible tube 201 is withdrawn into the treatment tool insertion channel251, the groove 3 may not be hooked at the end of the treatment toolinsertion channel 251.

As shown in FIGS. 16 and 17, a spoon tool 204A or a brush tool 204B maybe secured instead of the metal chip 204. With such configurations,tissues can be endoscopically collected from the branch tube located atdeep inside the bile duct or bronchial tubes.

Also in such a case, by injecting contrast medium through the connectionbarrel 212, the flexible tube 201 can be inserted into a desired tube,which cannot be observed by eyes, with monitoring X-ray images.

The tools for collecting tissues are generally provided with a sheathmade from metal coil having a tendency to be straighten. By employingthe above configurations as shown in FIGS. 16 and 17, the flexible tube201 can be inserted easily since it follows the curvature of the bileduct or bronchial tubes, and therefore, the flexible tube 201 can beinserted into a deep portion.

ELEVENTH-THIRTEENTH EMBODIMENTS

FIG. 18 is a cross-sectional side view of a distal end portion of abendable treatment tool according to a first embodiment of theinvention.

In FIG. 18, numeral 301 denotes a flexible tube, which is to be insertedin a treatment tool insertion channel. At the distal end of the flexibletube 301, a spoon tool 302, which is formed with a cutting edge at theperipheral thereof, for collecting human tissues is secured.

As the flexible tube 301, tetrafluoroethylene resin tube or polyethylenetube may be used. An outer diameter of the flexible tube isapproximately 1.5-2.5 mm and the length is 1-2 m.

At the distal end portion of the flexible tube 301, a pair of grooves303 a and 303 b, each having a V-shaped cross-section and extending in adirection perpendicular to the axis of the flexible tube 301, are formedwith a predetermined interval therebetween along the axis of theflexible tube 301.

Inside the flexible tube 301, an operation wire 304, which is formedfrom twisted stainless-steel wires, is inserted over the entire lengthof the flexible tube 301. The operation wire 304 is movable back andforth along the axis of the flexible tube 301. The operation wire 304can be operated arbitrarily from a proximal end (i.e., right-hand sidein FIG. 18) thereof.

The distal end 304 a of the operation wire 304 is secured to the spoontool by brazing or the like, thereby the distal end 4 a of the wire 304is secured to the distal end of the flexible tube 301. It should benoted that the distal end 304 a of the wire 304 may be directly securedonto the distal end of the flexible tube 301.

As shown in FIG. 18, the operation wire 304 runs out through the groove303 a and enters inside the flexible tube 301 through the groove 303 b.Between the grooves 303 a and 303 b, the operation wire 304 runs alongthe outer circumference of the flexible tube 301.

When the operation wire 304 is pulled at the proximal end side thereof(i.e., moved in the right-hand side in FIG. 18), as shown in FIG. 19,the distal end portion of the flexible tube 1 bends at the grooves 303 aand 303 b in a direction of a tissue-collecting surface 302 a side ofthe spoon tool 302.

When the operation wire 304 is pushed at the proximal end side (i.e.,moved in the left-hand side direction in FIG. 1), as shown in FIG. 20,the distal end portion of the flexible tube 1 bends, at the grooves 303a and 303 b, in a direction opposite to the tissue-collecting surface302 a of the spoon tool 302.

As described above, according to the embodiment, only by forming a pairof grooves 303 a and 303 b, the distal end portion of the flexible tube301 can be made bendable, without employing link members as in theconventional art.

FIG. 21 is a cross-sectional side view of a distal end portion of abendable treatment tool according to a second embodiment of theinvention. In this embodiment, two pairs of the grooves 303 a and 303 bare formed. The operation wire 304 is lead out from the grooves 303 aand inserted inside the flexible tube 301 through the grooves 303 b. Byforming a plurality of pairs of grooves 303 a and 303 b, the distal endportion of the flexible tube 301 can be bent smoothly at a relativelylarge radius of curvature.

FIG. 22 is a side view of a distal end portion of a bendable treatmenttool according to a third embodiment of the invention. In the thirdembodiment, at the distal end of the flexible tube 301, a brush tool 312is secured for collecting the human tissues. Further, in the thirdembodiment, the two pairs of the grooves 303 a and 303 b are formed atdifferent positions along the circumferential direction of the flexibletube 301.

According to this embodiment, if the operation wire 304 is pulled (i.e.,moved in the right-hand side in FIG. 22), the distal end portion of theflexible tube 1 is bent in a twisted direction as shown in FIG. 23 (theoperation wire 304 is omitted from the drawing for the sake ofsimplicity). Thus, the distal end portion of the flexible tube 301 maybe smoothly inserted in a three-dimensionally curved organs such as adeep portion of a bronchial tube.

FOURTEENTH-SEVENTEENTH EMBODIMENTS

FIG. 24 is a partially cross-sectional side view of a measurement toolfor an endoscope according to a first embodiment of the invention.

In FIG. 24, numeral 401 denotes a flexible tube, which is to be insertedin a treatment tool insertion channel. As the flexible tube 401,tetrafluoroethylene resin tube or polyethylene tube may be used. Anouter diameter of the flexible tube is approximately 1.5-2.5 mm and thelength is 1-2 m.

On a rear side with respect to the distal end of the flexible tube 401by 10-50 mm, a groove 403 traversing the flexible tube 1 in the diameterdirection, and having a V-shaped cross section is formed. Inside theflexible tube 1, an operation wire 402 formed of twisted stainless steelwires are inserted over the entire length thereof. The operation wire402 is movable in the axis of the flexible tube 401.

At the distal end of the flexible tube 401, a cylindrical metal chip 404having a through hole in the axial direction is secured. The distal endof the operation wire 402 is silver brazed to the metal chip 404,thereby the distal end of the operation wire 402 is secured to thedistal end of the flexible tube 401. It should be noted that the abovestructure is an exemplary structure, and the distal end of the operationwire 402 may be secured to the flexible tube 401 at any position on thedistal end side with respect to the groove 403.

On the outer surface of the flexible tube 401 on the distal end sideportion 401 a with respect to the groove 403, circular gradations 405are formed at a predetermined interval of, for example, 5 mm.Preferably, the graduations 405 are formed to have a color (e.g., blue)which can be clearly distinguished from the mucous membrane.

The proximal end of the flexible tube 401 is connected with an operationunit 410. Specifically, the operation unit includes a main barrel 411which is connected with the flexible tube 401. On a side portion of themain barrel 411, a connection barrel 412 is protruded. The connectionbarrel 412 communicates with the flexible tube 401, and a end portion ofthe connection barrel 412 defines an injection mouth 412 a. With thisconfiguration, by connecting an injector or the like (not shown) to theconnection barrel 412, through which water or any other liquid can befed in the flexible tube 401. Further, suction can be performed throughthe flexible tube 401 and the connection barrel 412.

The operation wire 402 runs straight through the main barrel 411, andthe proximal end of the operation wire 402 is connected with a fingerhook 414. The portion of the operation wire 402 from the main barrel 411to the finger hook 414, a stainless-steel reinforcement pipe 415 isprovided to cover the operation wire 402 to prevent the same frombending.

With the above-described configuration, by moving the finger hook 414back and forth with respect to the main barrel 11, the operation wire402 moves back and forth, along the axis, inside the flexible tube 401.In FIG. 24, 413 denotes an O-ring which is used for sealing a spaceinside the main barrel 411 and outside of the main barrel 411. TheO-ring 413 closely contacts the outer circumference of the reinforcementpipe 415.

With the above-described configuration, by moving the finger hook 414back and forth with respect to the main barrel 411, as shown in FIG. 25,the distal end portion 401 a of the flexible tube 401 is bent on thegroove 403 side at the groove 403. The maximum bending angle of thedistal end portion 401 a can be adjusted by the cross-sectional shape ofthe groove 403.

As shown in FIG. 26, by making the distal end portion 401 a from theinsertion channel 451 of the endoscope 450, and bending the distal endportion 401 a aside, the graduations 405 can be observed in anobservation field A. Thus, using the graduations 5, the size of anobject such as an ulcer can be measured.

When necessary, an injector may be connected to the connection barrel412 to feed water, thereby mucilaginous solution or blood on the mucousmembrane can be washed away with the water as shown in FIG. 27.

In this case, if the distal end portion 1 a of the flexible tube 401 isstraightened as shown in FIG. 28, part of the water may leak from thegroove 403. However, most of the water is ejected from the distal end ofthe flexible tube 401, and the mucilaginous solution or blood will bewashed away.

The present invention is not limited to the above-describedconfiguration, and can by modified in various ways. For example, thegroove 403 can be modified such that the bottom of the groove 403 may beformed to have a rounded portion as shown in FIG. 29. With thisconfiguration, the durability against repetitive bending will beimproved.

As shown in FIG. 30, the flexible tube 401 may be configured such thatthe metal chip 404 completely close the opening of the flexible tube 401at the distal end thereof. With this configuration, all the liquid fedfrom the connection barrel 412 will be ejected from the groove 403.

Optionally, as shown in FIG. 31, graduations 405M may be provided on theouter circumferential of the flexible tube 401 on the rear side withrespect to the groove 403. With this configuration, by bending thedistal end portion 1 a, and a length from the groove 403 to a proximalside portion of a lumen, in which the flexible tube 401 is inserted, canbe measured. In this case, if the color and/or thickness and/or numberof the graduations at each point is different from the graduation atanother point, measurement can be performed easily.

EIGHTEENTH EMBODIMENT

FIG. 32 is a cross-sectional side view showing an entire structure of acatheter for an endoscope according to a first embodiment of theinvention.

The catheter includes a flexible tube 501 which is to be inserted in atreatment tool insertion channel of an endoscope (not shown). Theflexible tube 501 is made of tetrafluoroethylene resin, inner/outerdiameters of which are approximately 1 mm/2 mm.

Inside the flexible tube 501, an operation wire 502 formed of twistedstainless-steel wires over the entire length of the flexible tube 501.The diameter of the operation wire 502 is sufficiently small so that itdoes not prevent flow of liquid inside the flexible tube 501. Theoperation wire 502 is movable along the axis of the flexible tube 501.

At a distal end portion of the flexible tube 501 (i.e., at a position1-5 cm spaced from the distal end of the flexible tube 1), a groove 505,which extends in a direction perpendicular to the axis of the flexibletube 501 and has a V-shaped cross section, is formed. The depth of thegroove 505 is set to traverse the inner diameter, and thus, thethickness of the flexible tube 1 remains without being formed withgroove 505.

Further, the bottom of the groove 505 is formed to have a curvedsurface. Therefore, the flexible tube 501 may not be cracked even if itis bent at the groove repeatedly. A pair of holes 503 are formed on theflexible tube 501 with the groove 504 located therebetween. Theoperation wire 502 is inserted through the holes 503 so that theoperation wire 502 is located outside the flexible tube 501 at a portionbetween the two holes 503.

The distal end of the operation wire 502 is silver brazed to a stopper506 which is made of, for example, stainless-steel. The stopper 506 isprovided at a position on the distal end side of the groove 505 of theflexible tube 501.

FIG. 33 is a cross-sectional view of the stopper 506 taken along lineB-B of FIG. 32. The stopper 506 is a pipe member which is inscribed inthe flexible tube 501. A portion of the stopper 506 at which theoperation wire 2 is secured is formed as a concave portion, and a liquidflowing path 507 is defined in the axial direction thereof.

As shown in FIG. 32, the distal end portion of the flexible tube 1 isconfigured such that the distal end side with respect to the stopper 506is tapered to have a smaller diameter at the portion closer to the end.With this configuration, the stopper 6 does not move freely to thedistal end portion. Accordingly, the stopper 506 is fixed in theflexible tube 501.

An operation unit 510 is connected to the proximal end of the flexibletube 501. A connection mouth 512 communicating the flexible tube isprotruded on a main barrel 511. By connecting an injector of the like tothe connection mouth 512, injection of chemicals or suction can beperformed. In FIG. 1, 514 denotes an O-ring for sealing. By fastening orreleasing a screw 515, the deformation amount of the O-ring 514 can beadjusted.

By moving a finger hook 513, which is connected to the proximal end ofthe operation wire 502, relative to the main barrel 511, the operationwire 502 moves back and forth along the axis of the flexible tube,thereby the distal end portion of the flexible tube can be bentarbitrarily.

FIG. 34 shows a cross-sectional side view of the flexible tube 501. Whenthe operation wire 502 is pulled at the operation unit 510, the distalend portion of the flexible tube 501 bends in a direction where thegroove 505 closes, as indicated by dotted lines.

If the operation wire 502 is pushed at the operation unit 510, as shownin FIG. 34, the distal end portion of the flexible tube 1 in a directionwhere the groove 505 opens wider, as indicated by solid lines in FIG.34.

With this configuration, a resistive force against the movement of thewire 502 is a force necessary for bending the flexible tube 1 at thegroove 505. Thus, even when the operation wire 502 is pushed, theflexible tube 501 can be bent.

As described above, according to the above-described embodiment, thedistal end portion of the flexible tube 501 can be bent in bothdirections at the position where the groove 505 is formed. Therefore,the flexible tube can be directed to the desired position easily.

NINETEENTH AND TWENTIETH EMBODIMENTS

FIG. 38 shows a partially cross-sectional side view of a cytodiagnosisbrush for an endoscope according to a first embodiment. In FIG. 38, 601denotes a flexible tube to be inserted in a treatment tool channel of anendoscope. The flexible tube 601 is made of, for example,tetrafluoroethylene resin.

At the proximal end of the flexible tube 601, a connection mouth piece610 is connected. At the distal end of the flexible tube 601, a brushshaft 611 provided with radially planted brush 612.

FIG. 36 shows a distal end portion of the flexible tube 601. The brush612 is provided at the distal end portion of the shaft 611, and theremaining portion of the shaft 611 is inserted in the flexible tube 601.The proximal end of the shaft 611 is secured with a stopper 602. Thestopper 602 is fixed to the distal end portion of the flexible tube 1 byheat-reducing the diameter of the flexible tube 601 at both sides of thestopper 602.

FIG. 37 shows a cross-sectional view taken along line C-C of FIG. 36.The stopper 602 is made of a stainless-steel pipe formed with a concaveportion, to which the proximal end of the shaft 611 is silver brazed.

An area of the stopper 602, which is not closed by the brush, defines aliquid path 603. That is, the proximal end side of the flexible tube 601communicates with the distal end side thereof without being closed bythe stopper 602.

Thus, when cleaning fluid or disinfecting fluid is injected to theflexible tube 1 through the connection mouth 310, the fluid passesthrough the liquid path and is fed out of the distal end of the flexibletube 601. Therefore, the flexible tube 601 can be cleaned and/ordisinfected over the entire length thereof, reliably and relativelyeasily.

FIG. 39 shows the cytodiagnosis brush for an endoscope according to asecond embodiment. In this embodiment, an operation wire 605 formed oftwisted stainless-steel wires are inserted in the flexible tube 601 fromthe proximal end to the distal end portion thereof.

The operation wire 605 has a sufficiently small diameter in comparisonto the inner diameter of the flexible tube 1 so that it does notobstruct the flow of liquid inside the flexible tube 601. The operationwire 5 is movable, in the flexible tube 601, in a direction of the axisof the flexible tube 601.

At a position close to the distal end of the flexible tube 601 (i.e.,1-5 cm from the distal end), a groove 604 having a V-shaped crosssection is formed.

The depth of the groove 604 is set to traverse the inner diameter of theflexible tube 601. Thus, a portion of the flexible tube 601 located atthe bottom of the V-shaped groove 4 remains uncut. Further, the bottomof the V-shaped groove 604 is formed to have a curved surface but not anedge. Therefore, even if the flexible tube 601 is repeatedly bent at thegroove 604, a crack or the like will not be formed on the flexible tube601.

As shown in FIG. 39, the flexible tube 601 is formed with a pair ofholes with the groove 604 located therebetween. The operation wire 605is inserted through the pair of holes 606 such that the operation wire605 is located outside the flexible tube 1 between the pair of holes606.

The distal end of the operation wire 605 is silver brazed to a stopper602 which is arranged, inside the flexible tube 601, at a position on adistal end side with respect to the groove 604. The proximal end of theshaft 611 of the brush is also silver brazed to the stopper 602.

To the proximal end of the flexible tube 601, an operation unit 620 isconnected. The operation unit 620 includes a main body 621 and aconnection mouth 10, which communicates with the flexible tube 601, isprotruded from the main body 621. By coupling an injector or the like tothe connection mouth 610, fluid can be injected inside the flexible tube601. In FIG. 39, 624 denotes an O-ring for sealing.

The proximal end of the operation wire 605 is connected to a finger hook623. By moving the finger hook 623 relative to the main body 621, theoperation wire 605 can be moved along the axis of the flexible tube 601,thereby bending the distal end portion of the flexible tube 601.

FIG. 40 shows a cross-sectional view of the distal end portion of theflexible tube 601. When the operation wire 605 is pulled at theoperation unit 620, the distal end portion of the flexible tube 601bends, at the groove 604, in a direction in which the V-shaped groove604 is closed as indicated by two-dotted lines in FIG. 40.

When the operation wire 5 is pushed at the operation unit 620, theflexible tube 1 is bent in a direction where the V-shaped groove 604opens wider, as indicated by solid lines in FIG. 40. With thisstructure, since the liquid path is defined and stopper does not blockthe flow of fluid, the entire length of the flexible tube 601 can becleaned and/or disinfected reliably and easily.

It should be noted that above-described structures are examples, andvarious modification can be made. For example, the stopper 602 may beformed as a hollow cylindrical member, and the shaft of the brush 611may be secured on the inner surface of the hollow-cylindrical stopper602.

TWENTY-FIRST AND TWENTY-SECOND EMBODIMENTS

FIG. 42 is a cross-sectional side view of a biopsy forceps according toa first embodiment of the invention. The biopsy forceps has a flexibletube 701 made of, for example, tetrafluoroethylene resin.

Inside the flexible tube 701, an operation wire 705 is inserted over theentire length of the flexible tube 701. The operation wire 705 ismovable in the flexible tube 701 in the axial direction thereof.Specifically, an operation unit is secured to the proximal end of theflexible tube 701, and the operation wire 705 is operated at theoperation unit (not shown).

At the distal end of the flexible tube 701, a support frame 703 isfixed. At the tip portion of the support frame 703, a pair of forcepscups are supported such that they are opened/closed about the rotationshaft 704.

Between the operation wire 705 and the forceps cups 702, a pantographtype link mechanism 706. By operating the operation wire 705, the pairof forceps cups 702 are opened (as indicated by two-dotted lines) orclosed (as indicated by solid lines) about the rotation shaft 704.

At a portion close to the distal end of the flexible tube 701 (e.g.,several millimeters to ten and several millimeters from the forcepscups), an incision 710 is formed from the outer surface of the flexibletube 701 along its diameter. The end of the incision 710 is located at aposition passed through the inside of the flexible tube 701, and theproximal end side portion of the flexible tube 701 and the distal endside portion thereof are connected by the remaining portion of theflexible tube 701 where the incision is formed.

When the operation wire 5 is pushed at the operation unit, the forceaffects the distal end portion of the flexible tube 701, the distal endportion of the flexible tube 701 bends in a direction where the incision710 opens, as shown in FIG. 41.

Therefore, as shown in FIG. 43, at a branched portion of a deepbronchial tube where the endoscope 750 is normally difficult to enter,by bending the distal end portion of the flexible tube 701, the biopsyforceps can be directed to a tube having the tumor 100.

Further, as shown in FIG. 44, by bending the distal end portion of theflexible tube 701 at the incision 100, the tissues can be collected withthe forceps cups 702 abutting against the root area of the tumor 100.Thus, accuracy in diagnosing the invasion area of malignant lesion isimproved.

It should be noted that the above-described configuration is an example,and various modification may be available. For example, as shown in FIG.45, the incision may be formed to have a V-shaped cross section, and theoperation wire 705 is located on the outside of the flexible tubebetween a pair of holes 711, which are formed to have the incision 710therebetween.

With this configuration, by operating the operation wire 705, the distalend portion of the flexible tube 1 can be directed in both sides (asindicated by two-dotted lines) with respect to a neutral position (whichis indicated by solid lines).

TWENTY-THIRD EMBODIMENT

FIG. 49 is a cross-sectional side view showing a distal end portion of ahigh-frequency cutting tool for an endoscope according to an embodimentof the invention.

The high-frequency cutting tool includes an electrically insulatingflexible tube 801 which is to be inserted in a treatment tool insertionchannel of an endoscope (not shown). The flexible tube 801 is made oftetrafluoroethylene resin, inner/outer diameters of which areapproximately 1 mm/2 mm.

Inside the flexible tube 801, a flexible conductive wire 802 formed oftwisted stainless-steel wires is inserted over the entire length of theflexible tube 801. The conductive wire 802 is movable along the axis ofthe flexible tube 801 at an operation unit (not shown). Further, theconductive wire 802 is connected to a high-frequency power supply codeat the operation unit, and the high-frequency power is arbitrarilyapplied.

At a distal end portion of the flexible tube 801 (i.e., at a position1-5 cm spaced from the distal end of the flexible tube 1), a groove 805,which extends in a direction perpendicular to the axis of the flexibletube 801 and has a V-shaped cross section, is formed. The depth of thegroove 805 is set to traverse the inner diameter, and thus, thethickness of the flexible tube 801 remains uncut.

Further, the bottom of the groove 5 is formed to have a curved surface.Therefore, the flexible tube 801 may not be cracked even if it is bentat the groove repeatedly. A pair of holes 803 are formed on the flexibletube 801 with the groove 804 located therebetween. The conductive wire802 is inserted through the holes 803 so that the conductive wire 802 islocated outside the flexible tube 801 at a portion between the two holes803.

The distal end portion of the flexible tube 801 is tapered (i.e., formedto have a smaller diameter at a distal end side). Inside the taperedportion of the flexible tube 801, a stopper 806, which is fixed on thedistal end of the conductive wire 802, is fitted in so that the stopperis fixed to the flexible tube 801.

By pulling the conductive wire 802 at the operation unit, the distal endportion of the flexible tube 801 is bent. Since the portion formed withthe groove 805 is much easier to bend than the other portion, bending isachieved mostly at the position where the groove 805 is formed, as shownin FIG. 50.

After the groove 805 is completely closed, the other portion starts tobend. However, in such a case, the force required for pulling theconductive wire 802 increases greatly, and therefore, the operator canrecognize the bending condition of the tool.

Thus, if the pulling operation of the conductive wire 802 is stoppedwhen the force necessary for pulling the conductive wire 802 increasesremarkably, the distal end portion of the flexible tube 801 is bent at apredetermined bending amount. Therefore, the human tissues can be cut ata desired depth A.

It should be noted that the cutting depth A can be adjusted by distancesP and Q (i.e., distances from the groove 805 and the holes 803).

Although twenty-three embodiments are described separately, any suitablecombination among the above-described embodiments and variation of thesame should also be the subject of the present invention.

The present disclosure relates to the subject matters contained inJapanese Patent Applications No. 2001-050545, filed on Feb. 26, 2001,No. 2001-051580, filed on Feb. 27, 2001, No. 2001-056076, filed on Mar.1, 2001, No. 2001-056212, filed on Mar. 1, 2001, No. 2001-196466, filedon Jun. 28, 2001, No. 2001-217503, filed on Jul. 18, 2001, and No.2001-217504, filed on Jul. 18, 2001, and No. 2001-218138, filed on Jul.18, 2001, which are expressly incorporated herein by reference in theirentireties.

1. A tubular treatment tool for an endoscope, comprising: a flexibletubular member, a groove traversing said flexible tubular member in adirection of a diameter of said flexible tubular member; an operationwire positioned within said flexible tubular member, said operation wirebeing movable relative to said flexible tubular member along an axis ofsaid flexible tubular member; and a tissue collecting device attached tothe distal end of said flexible tubular member, one circumferentialportion of a distal end of said operation wire being secured to an innercircumferential surface of the tissue collecting device by brazing and asecond circumferential portion of the distal end of said operation wireis not secured to the tissue collecting device, wherein a proximal endportion of the tissue collecting device is provided with protrudedportions having a wedge-shaped cross-section that prevents removal ofthe tissue collecting device from the flexible tubular member, whereinthe protruded portions are acuate, and wherein a gap exists between thesecond circumferential portion of the distal end of said operation wireand the inner circumferential surface of the tissue collecting device.2. The tubular treatment tool according to claim 1, wherein said groovehas a V-shaped cross section.
 3. The tubular treatment tool according toclaim 1, wherein the tissue collecting device is a spoon tool.
 4. Thetreatment tool according to claim 1, wherein the spoon tool comprises acutting edge.
 5. The treatment tool according to claim 1, wherein theone circumferential portion of the distal end of said operation wire issecured to the inner circumferential surface of the tissue collectingdevice at a side on which the groove is formed.